Matveenko, MariaBanwell, MartinWillis, Anthony2015-12-100040-4020http://hdl.handle.net/1885/51112The synthesis of the title compound [(-)-1] has been achieved, for the first time, by reacting the aryl boronic acid ester 4 with the aminoconduritol derivative 6 under Suzuki-Miyaura cross-coupling conditions then subjecting the product phenanthridinoneKeywords: benzene derivative; boronic acid derivative; bromide; isoenzyme; narciclasine; phenanthrene derivative; toluene dioxygenase; unclassified drug; article; biotransformation; cis isomer; crystal structure; deprotection reaction; drug structure; drug synthesi200810.1016/j.tet.2008.01.1132015-12-09